About This Role
We are seeking a highly skilled Medical Device Packaging Specialist to join our team.
This is an exciting opportunity for a seasoned professional to take on a key role in leading cross-functional projects, recommending new packaging materials and equipment, and ensuring compliance with regulations.
Main Responsibilities:
* Lead cross-functional projects for new product development and commercialization, and changes to existing products
* Recommend new packaging materials, equipment, and suppliers
* Develop and validate sterile packaging and labelling systems and equipment
* Ensure compliance with and monitor changes to packaging regulations
* Write and coordinate technical documentation, including design assurance documents, protocols, reports, procedures, specifications, work instructions, and original data
* Develop and validate test methods
* Source and validate packaging test equipment
* Identify and support cost savings opportunities
* Represent the organization at industry events (conferences, seminars, etc.)
* Educate the organization on packaging best practices
Requirements:
* Third Level Qualification (Science or Engineering Discipline)
* 6 Years Previous Experience in Sterile Packaging System Development and Validation